TY - JOUR
T1 - Chronic hepatitis C, depression and gender: a state of art
AU - Martin-Santos, Rocio
AU - Egmond, Elfi
AU - Cavero, Myriam
AU - Mariño, Zoe
AU - Subira, Susana
AU - Navines, Ricard
AU - Forns, Xavier
AU - Valdes, Manuel
PY - 2015/1/1
Y1 - 2015/1/1
N2 - © 2015, © Emerald Group Publishing Limited. Purpose – The purpose of this paper is to provide a comprehensive overview of the current knowledge regarding chronic hepatitis C (CHC) infection, antiviral therapy, depression, and gender. Design/methodology/approach – CHC and its treatment options were reviewed examining their relationship with depression and gender. Findings – CHC is a high prevalent chronic infection worldwide, being similar in men and women. However, the infection shows many gender differences in terms of innate response, genetic variability (i.e. IL-28B), route of transmission (i.e. intravenous drug use), disease progression (i.e. fibrosis), lifetime period (i.e. pregnancy), and risk factors (i.e. HIV). Both the hepatitis C infection and antiviral treatment (especially when using the pro-inflammatory cytokine interferon α), are highly associated with depression, where female gender constitutes a risk factor. It seems that the new direct-acting antiviral combinations produce fewer neuropsychiatric side effects. In fact, the presence of depression at baseline is no longer a limitation for the initiation of antiviral treatment. Antidepressant drugs have been recommended as current depression and prophylactic treatment in risk subgroups. However, caution should be exercised due to the risk of drug-drug interactions with some antiviral drugs. Women should be counselled prenatal, during and after pregnancy, taking into account the clinical situation, and the available evidence of the risks and benefits of antiviral and antidepressant treatments. Multidisciplinary approach shows cost-efficacy results. Originality/value – The paper clarifies the complex management of CHC therapy and the importance of individualizing treatment. The results also underline the need for an integrated multidisciplinary approach.
AB - © 2015, © Emerald Group Publishing Limited. Purpose – The purpose of this paper is to provide a comprehensive overview of the current knowledge regarding chronic hepatitis C (CHC) infection, antiviral therapy, depression, and gender. Design/methodology/approach – CHC and its treatment options were reviewed examining their relationship with depression and gender. Findings – CHC is a high prevalent chronic infection worldwide, being similar in men and women. However, the infection shows many gender differences in terms of innate response, genetic variability (i.e. IL-28B), route of transmission (i.e. intravenous drug use), disease progression (i.e. fibrosis), lifetime period (i.e. pregnancy), and risk factors (i.e. HIV). Both the hepatitis C infection and antiviral treatment (especially when using the pro-inflammatory cytokine interferon α), are highly associated with depression, where female gender constitutes a risk factor. It seems that the new direct-acting antiviral combinations produce fewer neuropsychiatric side effects. In fact, the presence of depression at baseline is no longer a limitation for the initiation of antiviral treatment. Antidepressant drugs have been recommended as current depression and prophylactic treatment in risk subgroups. However, caution should be exercised due to the risk of drug-drug interactions with some antiviral drugs. Women should be counselled prenatal, during and after pregnancy, taking into account the clinical situation, and the available evidence of the risks and benefits of antiviral and antidepressant treatments. Multidisciplinary approach shows cost-efficacy results. Originality/value – The paper clarifies the complex management of CHC therapy and the importance of individualizing treatment. The results also underline the need for an integrated multidisciplinary approach.
KW - Antidepressants
KW - Breastfeeding
KW - Chronic hepatitis C
KW - Depression
KW - Direct acting antivirals
KW - Drug-drug interactions
KW - HIV
KW - Inflammation
KW - Interferon α
KW - Pregnancy
KW - Risk factors
KW - Treatment
U2 - 10.1108/ADD-05-2015-0009
DO - 10.1108/ADD-05-2015-0009
M3 - Review article
SN - 1757-0972
VL - 8
SP - 193
EP - 210
JO - Advances in Dual Diagnosis
JF - Advances in Dual Diagnosis
IS - 4
ER -